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Collective Syntheses of 8-Oxoprotoberberines via Sequential In(OTf)3-Catalyzed Cyclization and Pd(OAc)2-Catalyzed Heck Coupling
The Journal of Organic Chemistry ( IF 3.3 ) Pub Date : 2023-05-12 , DOI: 10.1021/acs.joc.3c00419
Zenghui Sun 1, 2, 3 , Xinhang Zhang 1, 2, 3 , Jiayue Fu 1, 2, 3 , Lianjie Zhang 1, 2, 3 , Maosheng Cheng 1, 3 , Lu Yang 1, 2, 3 , Yongxiang Liu 1, 2, 3
Affiliation  

Six 8-oxoprotoberberines were synthesized collectively in four steps with acceptable yields (14–19%), of which the products 8-oxopalmatine, 8-oxopseudopalmatine, 8-oxoberberine, and 8-oxopseudoberberine come from nature. The synthetic route was featured with the In(OTf)3-catalyzed cyclization and Heck coupling. Moreover, the syntheses of the natural products berberine, canadine, and iambertine were achieved via various reductions from 8-oxoberberine, which provided a concise approach to the syntheses of this kind of alkaloids.

中文翻译:

通过顺序 In(OTf)3 催化环化和 Pd(OAc)2 催化 Heck 偶联集体合成 8-Oxoprotoberberines

共分四步合成了 6 种 8-氧代原小檗碱,收率可接受 (14-19%),其中产物 8-氧代棕榈碱、8-氧代假小檗碱、8-氧代小檗碱和 8-氧代假小檗碱来自自然界。该合成路线以In(OTf) 3催化环化和Heck偶联为特点。此外,通过8-氧代小檗碱的各种还原反应,合成了天然产物小檗碱、加拿大黄连素和黄柏碱,为这类生物碱的合成提供了一种简洁的方法。
更新日期:2023-05-12
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